Does OFATUMUMAB Cause Device issue? 259 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 259 reports of Device issue have been filed in association with OFATUMUMAB (ARZERRA). This represents 0.9% of all adverse event reports for OFATUMUMAB.
259
Reports of Device issue with OFATUMUMAB
0.9%
of all OFATUMUMAB reports
0
Deaths
12
Hospitalizations
How Dangerous Is Device issue From OFATUMUMAB?
Of the 259 reports, 12 (4.6%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OFATUMUMAB. However, 259 reports have been filed with the FAERS database.
What Other Side Effects Does OFATUMUMAB Cause?
Fatigue (5,202)
Headache (4,430)
Pain (3,382)
Chills (3,372)
Pyrexia (3,370)
Influenza like illness (2,727)
Nausea (1,688)
Multiple sclerosis relapse (1,525)
Covid-19 (1,435)
Asthenia (1,393)
What Other Drugs Cause Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which OFATUMUMAB Alternatives Have Lower Device issue Risk?
OFATUMUMAB vs OFLOXACIN
OFATUMUMAB vs OLANZAPINE
OFATUMUMAB vs OLANZAPINE\SAMIDORPHAN L-MALATE
OFATUMUMAB vs OLAPARIB
OFATUMUMAB vs OLARATUMAB